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941.
珠宝市场上见到的大尺寸珊瑚有增多趋势,这类珊瑚多为珊瑚小料和胶结物拼合而成,前人研究未对其鉴定特征进行系统总结.笔者结合长期宝石检测工作认识,对目前市场上常见的两类拼合珊瑚的鉴定特征进行了系统研究和阐述.其中,一类拼合珊瑚由珊瑚小料和胶结物组成,另一类拼合珊瑚由珊瑚小料、人工胎体材料和胶结物组成.放大检查和紫外荧光观察发现,拼合部位的胶结物、胎体材料与主体红珊瑚在外观及发光性特征上存在差异明显;红外光谱测试结果进一步确定胶结物的主要成分为甲基丙烯酸甲酯和环氧树脂,部分拼合珊瑚依附的胎体材料主要为醇酸树脂(掺有碳酸盐粉末)和氰基丙烯酸乙酯.结果表明,放大检查、紫外荧光观察和红外光谱测试的综合运用,能够快速、准确、有效地鉴别拼合珊瑚. 相似文献
942.
943.
Adsorption behaviors of Cd^2+ on Fe2O3/MnO2 and the effects of coexisting ions under alkaline conditions 总被引:2,自引:0,他引:2
This study describes the adsorption features of cadmium on Fe2O3 and MnO2 in alkaline saline conditions. The adsorption reached equilibrium in 6 hours under alkaline conditions. The absorption of cadmium on Fe2O3 and MnO2 was consistent with Freundlich absorption isotherms, and the corresponding adsorption capacities were 16.3 and 16.7 mg·g-1, respectively. Moreover, the adsorption quantity of cadmium on Fe2O3 and MnO2 rose with increasing pH from acidic to neutral, and reached the maximum at pH= 9. The coexisting chlorides reduced the adsorption capacity of Fe2O3 and MnO2. The influence intensities of different cations follow the order of CaCl2>>KCl>NaCl. However, the influence of sodium salts on the capacities of Fe2O3 and MnO2 to adsorb cadmium appeared more complicated: the relatively low concentrations of sodium salts could reduce the adsorption capacity; with increasing concentrations of sodium salts, e.g. NaCl and NaNO3. The adsorption capacity decreased continually. Moreover, due to the competition adsorption and precipitation effects, the adsorption capabilities of Na2CO3, NaH2PO4 and Na2HSO4 could also be reduced and cadmium concentrations in the solution were reduced as well. 相似文献
944.
945.
[摘要]分别以铜327郾4 nm 和249郾2nm、铅283郾3 nm 和261郾4nm、锌307郾6nm 次灵敏线为分析线,
火焰原子吸收光谱法测定了高品位矿石中铜、铅、锌的含量。考察了高品位矿石基体及主要杂质的干扰
情况,结果表明,铜、锌质量浓度小于2 mg/ ml 时,对铅的测定无干扰;铅质量浓度小于2 mg/ ml 时,对铜
测定无干扰,其质量浓度小于0郾5mg/ ml 时,对锌测定无干扰;测定溶液中主要杂质铁、钴、镍、钙、镁质量
浓度在1mg/ ml,铝、硅质量浓度在0郾2mg/ ml 对测定无干扰。铜铅锌的质量浓度分别在0 ~ 1000滋g/ ml
范围内呈良好的线性关系。方法的精密度(RSD,n=5) 小于5%,加标回收率在98郾91% ~ 101郾08%,测
定铜铅锌矿石国家标准物质,结果与标准值相符。 相似文献
946.
Well-resolved Raman spectra of examples of nitrogen-containing compounds were detected using a portable Raman instrument (Ahura First Defender XL) outdoors at a low temperature of −15 °C at an altitude of 2860 m (Pitztall, Austria). The portable Raman spectrometer tested here is equipped with a 785 nm diode laser and fixed frontal probe. Solid forms of formamide, urea, 3-methylpyridine, aniline, indene, 1-(2-aminoethyl)piperazine, benzofuran and indoline were detected unambiguously under field high-mountain conditions. The main Raman features (strong, medium and partially weak bands) were observed at their correct wavenumber positions (spectral resolution 7-10 cm−1) in the range 200-2000 cm−1. The results obtained demonstrate the possibility of applying a miniaturised Raman spectrometer as key instrument for investigating the presence of nitrogen-containing organic compounds and biomolecules under low temperature field conditions. Within the payload designed by ESA and NASA for future missions focusing not only on Mars, Raman spectroscopy will be an important non-destructive analytical tool for the in-situ identification of both organic and inorganic compounds relevant to life detection on planetary surfaces or near sub-surfaces. 相似文献
947.
Paul F. Schofield Andrew D. Smith J. Frederick W. Mosselmans Hendrik Ohldag Andreas Scholl Simone Raoux Gordon Cressey Barbara A. Cressey Paul D. Quinn Caroline A. Kirk Simon C. Hogg 《Geostandards and Geoanalytical Research》2010,34(2):145-159
This work describes the application of microfocus X-ray absorption spectroscopy (XAS) and X-ray photo-emission electron microscopy (XPEEM) to the study of the complex mineralogical intergrowths within the Santa Catharina meteorite. The Santa Catharina meteorite of this study (BM52283 from the meteorite collection of the Natural History Museum, London, UK) primarily comprises a taenite bulk host phase (Fe:Ni ratio = 70.9 ± 0.8%:29.1 ± 0.8%) with a set of oxide-bearing cloudy zone textured regions (Fe:Ni:O ratio = 40.4 ± 0.3%:49.0 ± 0.7%:10.6 ± 0.8% at the core and Fe:Ni:O ratio = 34.4 ± 1.5%:42.7 ± 0.6%:22.9 ± 1.8% towards the rims) and numerous schreibersite (Fe:Ni:P ratio = 38.6 ± 1.6%:38.4 ± 0.9%:23.0 ± 0.5%) inclusions. Between the schreibersite and the taenite are rims up to 50 μm across of Ni-rich kamacite (Fe:Ni ratio = 93.4 ± 0.4%:6.6 ± 0.5%). No chemical zoning or spatial variations in the Fe and Ni speciation was observed within either the schreibersite or the kamacite phases. The oxide-bearing cloudy zone textured regions mostly comprise metallic Fe–Ni alloy, predominantly tetrataenite. Within the oxide phases, the Fe is predominantly, but not entirely, tetrahedrally co-ordinated Fe3+ and the Ni is octahedrally co-ordinated Ni2+. Structural analysis supports the suggestion that non-stoichiometric Fe2NiO4 trevorite is the oxide phase. The trevorite:tetrataenite ratio increases at the edges of the oxide-bearing cloudy zone textured regions indicating increased oxidation at the edges of these zones. The spatial resolution of the XPEEM achieved was between 110 and 150 nm, which precluded the study of either the previously reported ∼ 10 nm precipitates of tetrataenite within the bulk taenite or any antitaenite. 相似文献
948.
949.
Y. Fenner M. T. Murphy B. K. Gibson 《Monthly notices of the Royal Astronomical Society》2005,358(2):468-480
At redshifts z abs ≲ 2 , quasar absorption-line constraints on space–time variations in the fine-structure constant, α, rely on the comparison of Mg ii and Fe ii transition wavelengths. One potentially important uncertainty is the relative abundance of Mg isotopes in the absorbers, which, if different from solar, can cause spurious shifts in the measured wavelengths and, therefore, α. Here we explore chemical evolution models with enhanced populations of intermediate-mass (IM) stars, which, in their asymptotic giant branch phase, are thought to be the dominant factories for heavy Mg isotopes at the low metallicities typical of quasar absorption systems. By design, these models partially explain recent Keck/HIRES evidence for a smaller α in z abs < 2 absorption clouds than on Earth. However, such models also overproduce N, violating observed abundance trends in high- z abs damped Lyman-α (DLA) systems. Our results do not support the recent claim of Ashenfelter et al. that similar models of IM-enhanced initial mass functions (IMFs) may simultaneously explain the HIRES varying-α data and DLA N abundances. We explore the effect of the IM-enhanced model on Si, Al and P abundances, finding it to be much less pronounced than for N. We also show that the 13 C/12 C ratio, as measured in absorption systems, could constitute a future diagnostic of non-standard models of the high-redshift IMF. 相似文献
950.
M. Viel E. Branchini R. Cen J. P. Ostriker S. Matarrese P. Mazzotta B. Tully 《Monthly notices of the Royal Astronomical Society》2005,360(3):1110-1122
We present a simple method for tracing the spatial distribution and predicting the physical properties of the Warm–Hot Intergalactic Medium (WHIM), from the map of galaxy light in the Local Universe. Under the assumption that biasing is local and monotonic we map the ∼2 h −1 Mpc smoothed density field of galaxy light into the mass-density field, from which we infer the spatial distribution of the WHIM in the Local Supercluster. Taking into account the scatter in the WHIM density–temperature and density–metallicity relation, extracted from the z = 0 outputs of high-resolution and large-box-size hydrodynamical cosmological simulations, we are able to quantify the probability of detecting WHIM signatures in the form of absorption features in the X-ray spectra, along arbitrary directions in the sky. To illustrate the usefulness of this semi-analytical method we focus on the WHIM properties in the Virgo cluster region. 相似文献